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Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indic
Recalled September 1, 2021 · FDA recall Z-2286-2021 · Cardinal Health
Hazard
Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe. · FDA Class I
Units
267,217,860 eaches in total
Sold at
US Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY.
Description
Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.
Product
Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.
Manufacturer(s)
Cardinal Health
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →